N-methyl-D-aspartate receptor blockade during development induces short-term but not long-term changes in c-Jun and parvalbumin expression in the rat cervical spinal cord

Exp Neurol. 2001 Aug;170(2):380-4. doi: 10.1006/exnr.2001.7720.

Abstract

During postnatal development, N-methyl-D-aspartate receptor (NMDA-R) expression progressively decreases in ventral and deep dorsal horns. This transient expression might play a role in activity-dependent development of segmental circuitry. NMDA-Rs were blocked unilaterally in the lower cervical spinal cord using Elvax implants that released the NMDA-R antagonist MK-801 maximally over a 2-week period from postnatal day 7 (P7) onward. At P14, the ratio of c-Jun immunoreactive motoneurons ipsilateral/contralateral to the implants was significantly increased and the ratio of parvalbumin immunoreactive neurons decreased, compared to control implants. However, at P84, MK-801-treated and control spinal cords appeared the same. Therefore, NMDA-R blockade during development only transiently altered expression of activity-dependent proteins in the spinal cord, unlike lesions to the developing motor cortex, which we have previously shown to have a permanent effect.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging
  • Animals
  • Animals, Newborn
  • Dizocilpine Maleate / administration & dosage
  • Dizocilpine Maleate / pharmacology*
  • Drug Implants
  • Functional Laterality
  • Genes, jun
  • Motor Neurons / cytology
  • Motor Neurons / drug effects
  • Motor Neurons / physiology
  • Parvalbumins / analysis
  • Parvalbumins / metabolism*
  • Polyvinyls
  • Proto-Oncogene Proteins c-jun / analysis
  • Proto-Oncogene Proteins c-jun / metabolism*
  • Rats
  • Rats, Wistar
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors*
  • Spinal Cord / drug effects*
  • Spinal Cord / growth & development
  • Spinal Cord / physiology

Substances

  • Drug Implants
  • Parvalbumins
  • Polyvinyls
  • Proto-Oncogene Proteins c-jun
  • Receptors, N-Methyl-D-Aspartate
  • ethylenevinylacetate copolymer
  • Dizocilpine Maleate